Search results for "CRYSTAL STRUCTURE"

showing 10 items of 15036 documents

Crystal structure of diethyl 2-amino-5-{4-[bis-(4-methyl-phen-yl)amino]-benzamido}-thio-phene-3,4-di-carboxyl-ate.

2019

The title compound forms a head-to-head centrosymmetric dimer, involving a pair of inter­molecular N—H⋯O hydrogen bonds. It also forms two intra­molecular bonds between its amine and amide and the ester carbonyl groups.

inorganic chemicalscrystal structureintra- and intermolecular bondingThio-hydrogen-bonded dimerCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistryResearch Communicationslcsh:Chemistrychemistry.chemical_compoundAmideGeneral Materials SciencePhene010405 organic chemistryHydrogen bondRegioselectivityGeneral ChemistryCondensed Matter Physics3. Good health0104 chemical scienceslcsh:QD1-999chemistryintra- and inter­molecular bondingAmine gas treatingActa crystallographica. Section E, Crystallographic communications
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CCDC 1952457: Experimental Crystal Structure Determination

2020

Related Article: Francisco Estevan, Marta Feliz|2020|Dalton Trans.|49|4528|doi:10.1039/C9DT04821A

iodo-bis[(RR)-11'-(12-phenylene)bis(25-dimethylphospholane)]-iron iodide monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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The S … Hal and Se … Hal chalcogen bonding in a series of thiourea, selenourea and their derivatives

2021

The chalcogen bonding (ChB) in a series of thiourea, selenourea and their derivatives has been investigated in the present paper. Thus, selenourea and dimethylselenourea undergo dimerization and trimerization processes in the presence of various halogen species (1–5). Selenourea and dimethylselenourea form trimers 3–4 in the presence of lighter halogens (chlorine and bromine) through Se⋯Se chalcogen bonding. When moving to heavier halogen (iodine), the dimers 1–2 are formed. Thiourea and its derivatives also tend to make very strong S⋯S bonds and form dimers in the case of lighter halogens chlorine and bromine (compounds 6–7). However, the monomers separated by the iodine species are formed…

kemiaSelenoureachemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesInorganic Chemistryjodichemistry.chemical_compoundChalcogenkemialliset sidoksetklooriPolymer chemistryMaterials ChemistryChlorinechalcogen bondingbromiPhysical and Theoretical ChemistryselenoureathioureaBrominehalogeenitChemistry021001 nanoscience & nanotechnologyCondensed Matter Physicshalogen0104 chemical sciencesElectronic Optical and Magnetic MaterialsMonomerThioureaHalogenCeramics and Composites0210 nano-technology
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Synthesis of a Novel Hydrazone of Thieno[2,3-d]pyrimidine Clubbed with Ninhydrin: X-ray Crystal Structure and Computational Investigations

2023

The novel hydrazone-containing thieno[2,3-d]pyrimidine, namely, N′-(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)-2-(4-oxo-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-3(4H)-yl)acetohydrazide 4 was synthesized in a very good yield from the reaction of the triketoester 1 or ninhydrin 2 with the exocyclic acetohydrazide 3 in methanol. Good-quality crystals of 4 were obtained by recrystallization of the compound from the DMF/MeOH solvent mixture. The target product 4 crystallized in the triclinic crystal system and P-1 space group. The topology analysis of molecular packing indicated that the H…H (30.4%), O…H (22.0%) and H…C (17.0%) contacts are the most dominant i…

kemiallinen synteesiGeneral Chemical EngineeringX-ray crystal structureCondensed Matter Physicsthieno[23-d]pyrimidinethieno[23-<i>d</i>]pyrimidineHirshfeldInorganic Chemistryhydrazonex-ray crystal structureGeneral Materials Scienceninhydrinheterosykliset yhdisteetCrystals
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Optimizing the SYBR green related cyanine dye structure to aim for brighter nucleic acid visualization

2022

In recent years, the studies of RNA and its use for the development of RNA based vaccines have increased drastically. Although cyanine dyes are commonly used probes for studying nucleic acids, in a wide range of applications, there is still a growing need for better and brighter dyes. To meet this demand, we have systematically studied the structure of SYBR green-related cyanine dyes to gain a deeper understanding of their interactions with biomolecules especially how they interact with nucleic acids and the structural components which makes them strongly fluorescent. Herein, five new dyes were synthesized, and their photophysical properties were evaluated. Observations of photophysical cha…

kemiallinen synteesiväriaineetProcess Chemistry and TechnologyGeneral Chemical Engineeringtiheysfunktionaaliteoriafluoresenssinukleiinihapotmolecular dockingcyanine dyeX-ray crystal structureDFT calculationstestausbiomolekyylitnucleic acidfluorescent probesyaniiniväriaineetröntgenkristallografiaDyes and Pigments
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Extended Assemblies of Ru(bpy)(CO)2X2 (X = Cl, Br, I) Molecules Linked by 1,4-Diiodotetrafluoro-Benzene (DITFB) Halogen Bond Donors

2019

The ruthenium carbonyl compounds, Ru(bpy)(CO)2X2 (X = Cl, Br or I) act as neutral halogen bond (XB) acceptors when co-crystallized with 1,4-diiodotetrafluoro-benzene (DITFB). The halogen bonding strength of the Ru-X&sdot

kemialliset sidoksetcrystal structurebipyridinelcsh:QD901-999halogen bondcarbonyllcsh:CrystallographyorganometalliyhdisteetkiteetrutheniumCrystals
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Structural analysis of two foldamer-type oligoamides – the effect of hydrogen bonding on solvate formation, crystal structures and molecular conforma…

2012

Author's Final draft The crystal structures and molecular conformations of two foldamer-type oligoamides were analyzed. One polymorphic form and seven solvates were found for N¹,N³-bis(2-benzamidophenyl)benzene-1,3-dicarboxamide (the benzene variant), and two polymorphic forms and six solvates for N²,N⁶-bis(2-benzamidophenyl)pyridine-2,6-dicarboxamide (the pyridine variant). Three crystal structures of the benzene variant and seven structures of the pyridine variant were solved using single crystal X-ray diffraction. The crystal structures showed that the different modes of intramolecular hydrogen bonding strongly affect the conformation and folding of the molecules, which is most evidently…

kristallografiafoldameeriHydrogen bondStereochemistryFoldamerGeneral ChemistryCrystal structurekidetiedeCondensed Matter PhysicsoligoamideFolding (chemistry)chemistry.chemical_compoundCrystallographychemistryoligoamidifoldamerIntramolecular forcePyridineMoleculeGeneral Materials Scienceta116Single crystalCrystEngComm
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CCDC 1053707: Experimental Crystal Structure Determination

2015

Related Article: Jérôme Bayardon , Julie Bernard , Emmanuelle Rémond , Yoann Rousselin , Raluca Malacea-Kabbara , and Sylvain Jugé|2015|Org.Lett.|17|1216|doi:10.1021/acs.orglett.5b00167

lambda5-Boranyl(ferrocenyl)phenyl(2-(4455-tetramethyl-132-dioxaborolan-2-yl)phenyl)phosphoraneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Intermolecular hydrogen bonding in isostructural pincer complexes [OH-(t-BuPOCOPt-Bu)MCl] (M = Pd and Pt)

2019

In the crystal structure of the isostructural title compounds, namely {2,6-bis[(di-tert-butylphosphanyl)oxy]-4-hydroxyphenyl}chloridopalladium(II), [Pd(C22H39O3P2)Cl], 1, and {2,6-bis[(di-tert-butylphosphanyl)oxy]-4-hydroxyphenyl}chloridoplatinum(II), [Pt(C22H39O3P2)Cl], 2, the metal centres are coordinated in a distorted square-planar fashion by the POCOP pincer fragment and the chloride ligand. Both complexes form strong hydrogen-bonded chain structures through an interaction of the OH group in the 4-position of the aromatic POCOP backbone with the halide ligand. © 2019.

lcsh:Chemistrycrystal structurelcsh:QD1-999pincer complexesplatinum540palladiumhydrogen bondingActa Crystallographica Section E: Crystallographic Communications
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Crystal structure of a new spiro-polytetrahydrofuran compound with translational pseudosymmetry: rac-(2S,2′S,5′R)-2-methyl-5′-[(1R,2R,5S,5′R)-1,4,4,5…

2017

The title compound, C22H34O6, is a product of oxidation of squalene with the catalytic system RuO4(cat.)/NaIO4. The asymmetric unit contains two crystallographically independent molecules of very similar geometry approximately related by the non-crystallographic translation vector c/2. As a consequence, the average diffracted intensity in the hkl layers with odd l is systematically lower than in the layers with even l. In one molecule, the lactone ring and part of the adjacent tetrahydrofuran ring are disordered over two orientations with refined occupancy ratio of 0.831 (10):0.169 (10). The crystal structure is mainly governed by van der Waals forces.

lcsh:Chemistrycrystal structurelcsh:QD1-999pseudosymmetrypoly-THF compoundsspiro-compoundspseudotranslationActa Crystallographica Section E: Crystallographic Communications
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